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利用 InS/锐钛矿/Rutile TiO2 双倾斜异质结纳米树枝状阵列光阳极实现环保且高效的太阳能水分解。

Toward Eco-Friendly and Highly Efficient Solar Water Splitting Using InS/Anatase/Rutile TiO Dual-Staggered-Heterojunction Nanodendrite Array Photoanode.

机构信息

Department of Chemical Engineering, National Cheng Kung University , Tainan 701, Taiwan.

出版信息

ACS Appl Mater Interfaces. 2018 Jan 31;10(4):3714-3722. doi: 10.1021/acsami.7b19139. Epub 2018 Jan 16.

Abstract

The TiO-based heterojunction nanodendrite (ND) array composed of anatase nanoparticles (ANPs) on the surface of the rutile ND (RND) array is selected as the model photoanode to demonstrate the strategies toward eco-friendly and efficient solar water splitting using neutral electrolyte and seawater. Compared with the performances in alkaline electrolyte, a non-negligible potential drop across the electrolyte as well as impeded charge injection and charge separation is monitored in the ANP/RND array photoanode with neutral electrolyte, which are, respectively, ascribed to the series resistance of neutral electrolyte, the fundamentally pH-dependent water oxidation mechanism on TiO surface, as well as the less band bending at the interface of TiO and neutral electrolyte. Accordingly, a TiO-based dual-staggered heterojunction ND array photoanode is further designed in this work to overcome the issue of less band bending with the neutral electrolyte. The improvement of charge separation efficiency is realized by the deposition of a transparent InS layer on the ANP/RND array photoanode for constructing additional staggered heterojunction. Under illumination of AM 1.5G (100 mW cm), the improved photocurrent densities acquired both in neutral electrolyte and seawater at 1.23 V vs reversible hydrogen electrode (RHE), which approach the theoretical value for rutile TiO, are demonstrated in the dual-staggered-heterojunction ND array photoanode. Faradaic efficiencies of ∼95 and ∼32% for solar water oxidation in neutral electrolyte and solar seawater oxidation for 2 h are acquired at 1.23 V vs RHE, respectively.

摘要

基于 TiO2 的杂化纳米枝晶(ND)阵列由锐钛矿 ND(RND)阵列表面上的锐钛矿纳米颗粒(ANP)组成,被选为模型光阳极,用于展示使用中性电解质和海水进行环保高效太阳能分解水的策略。与在碱性电解质中的性能相比,在中性电解质中,在 ANP/RND 阵列光阳极中监测到电解质中相当大的电位降以及阻碍电荷注入和电荷分离,这分别归因于中性电解质的串联电阻、TiO2 表面上基本依赖 pH 的水氧化机制以及 TiO2 和中性电解质界面处的能带弯曲较小。因此,本工作进一步设计了基于 TiO2 的双交错异质结 ND 阵列光阳极,以克服中性电解质中能带弯曲较小的问题。通过在 ANP/RND 阵列光阳极上沉积透明 InS 层来构建额外的交错异质结,实现了电荷分离效率的提高。在 AM 1.5G(100 mW cm)照射下,在中性电解质和海水中在 1.23 V 相对于可逆氢电极(RHE)获得了改进的光电流密度,接近锐钛矿 TiO2 的理论值,在双交错异质结 ND 阵列光阳极中得到了证明。在 1.23 V 相对于 RHE 下,在中性电解质中进行太阳能水氧化的法拉第效率约为 95%,在太阳能海水中氧化 2 h 的法拉第效率约为 32%。

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